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Diabetic retinopathy: a comprehensive update on in vivo, in vitro and ex vivo experimental models

Lookup NU author(s): Evon Low

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

© 2023, BioMed Central Ltd., part of Springer Nature. Diabetic retinopathy (DR), one of the leading causes of visual impairment and blindness worldwide, is one of the major microvascular complications in diabetes mellitus (DM). Globally, DR prevalence among DM patients is 25%, and 6% have vision-threatening problems among them. With the higher incidence of DM globally, more DR cases are expected to be seen in the future. In order to comprehend the pathophysiological mechanism of DR in humans and discover potential novel substances for the treatment of DR, investigations are typically conducted using various experimental models. Among the experimental models, in vivo models have contributed significantly to understanding DR pathogenesis. There are several types of in vivo models for DR research, which include chemical-induced, surgical-induced, diet-induced, and genetic models. Similarly, for the in vitro models, there are several cell types that are utilised in DR research, such as retinal endothelial cells, Müller cells, and glial cells. With the advancement of DR research, it is essential to have a comprehensive update on the various experimental models utilised to mimic DR environment. This review provides the update on the in vitro, in vivo, and ex vivo models used in DR research, focusing on their features, advantages, and limitations.


Publication metadata

Author(s): Sadikan MZ, Abdul Nasir NA, Lambuk L, Mohamud R, Reshidan NH, Low E, Singar SA, Mohmad Sabere AS, Iezhitsa I, Agarwal R

Publication type: Review

Publication status: Published

Journal: BMC Ophthalmology

Year: 2023

Volume: 23

Online publication date: 19/10/2023

Acceptance date: 26/09/2023

ISSN (electronic): 1471-2415

Publisher: BioMed Central Ltd

URL: https://doi.org/10.1186/s12886-023-03155-1

DOI: 10.1186/s12886-023-03155-1

Data Access Statement: Not applicable.


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